Congenital midline cervical cleft: case report and review of the English language literature.

abstract：:Dyshidrotic eczema is one of the rare cutaneous adverse effects of intravenous immunoglobulin therapy, usually seen in adults. We herein report the first pediatric case of severe dyshidrotic eczema occurring after intravenous immunoglobulin therapy for Kawasaki syndrome. ...

journal_title：Pediatric dermatology

authors： Shiraishi T,Yamamoto T

更新日期：2013-05-01 00:00:00

abstract：:Cranioectodermal dysplasia is a rare syndrome characterized by craniofacial and skeletal anomalies and ectodermal dysplasia. Life-threatening associated conditions (i.e., kidney failure and abnormal regulation of the parathyroid-bone axis) can also develop. We report a patient whose features are suggestive of an inapp...

journal_title：Pediatric dermatology

authors： Zannolli R,Mostardini R,Carpentieri ML,Gatti MG,Galluzzi P,Terrosi Vagnoli P,Giorgetti R,Calvieri S,Morgese G

更新日期：2001-07-01 00:00:00

abstract：:We present a 16-year-old girl with a 4-year history of chronic persistent erythema nodosum. Recurrently low serum iron values suggested the possibility of a malabsorption syndrome. The presence of antitransglutaminase and antiendomysium antibodies and the jejunal biopsy specimen findings showed an underlying celiac di...

journal_title：Pediatric dermatology

authors： Bartyik K,Várkonyi A,Kirschner A,Endreffy E,Túri S,Karg E

更新日期：2004-05-01 00:00:00

abstract：:Benign cephalic histiocytosis is a rare skin condition consisting of small tan papules on the face and upper trunk that is believed not to be associated with internal organ involvement. The infiltrating histiocytes are not Langerhans' cells (LCs). We report a 5-year-old girl who presented with diabetes insipidus 1 yea...

journal_title：Pediatric dermatology

authors： Weston WL,Travers SH,Mierau GW,Heasley D,Fitzpatrick J

更新日期：2000-07-01 00:00:00

abstract：:We cared for 124 pediatric patients with a histologic diagnosis of Langerhans' cell histiocytosis (histiocytosis X) over a period of 14 years. Clinical, laboratory, and radiographic findings were analyzed. The most frequent manifestations were bone lesions, lymph node involvement, and skin infiltration. Liver disease ...

journal_title：Pediatric dermatology

authors： Rivera-Luna R,Martinez-Guerra G,Altamirano-Alvarez E,Martinez-Avalos A,Cardenas-Cardoz R,Ayon-Cardenas A,Ruiz-Maldonado R,Lopez-Corella E

更新日期：1988-08-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Loose anagen syndrome (LAS) is a disorder of abnormal anchorage of the hair to the scalp. Its symptoms include an inability to grow hair long and hair that is easily pulled out. METHODS:We conducted a retrospective chart review of patients with LAS over the last 10 years at the Children's Hospita...

journal_title：Pediatric dermatology

authors： Swink SM,Castelo-Soccio L

更新日期：2016-09-01 00:00:00

abstract：:Little is known about pediatricians' counseling and clinical practices to reduce skin cancer risk among their patients. Thus our objectives were to characterize skin cancer preventive counseling and clinical practices in a sample of pediatricians and identify correlates of these practices. Physicians practicing genera...

journal_title：Pediatric dermatology

authors： Gritz ER,Tripp MK,de Moor CA,Eicher SA,Mueller NH,Spedale JH

更新日期：2003-01-01 00:00:00

abstract：:We evaluated the prevalence of acanthosis nigricans among urban youth. Youth (7-17 years) at nine pediatric practices completed surveys on demographics and family history of diabetes and had weight and height measured. Acanthosis nigricans was scored and digital photography of the neck performed. A total of 618 youth ...

journal_title：Pediatric dermatology

authors： Brickman WJ,Binns HJ,Jovanovic BD,Kolesky S,Mancini AJ,Metzger BE,Pediatric Practice Research Group.

更新日期：2007-11-01 00:00:00

abstract：:Trisomy 13, or Patau syndrome, is a chromosomal disorder that can occur in complete, partial, or mosaic forms. Mosaicism is observed in 6% of individuals with trisomy 13 and, in contrast to the complete form, has wide phenotypic variability, longer survival, and in some patients an unusual skin pigmentary pattern simi...

journal_title：Pediatric dermatology

authors： González-del Angel A,Estandia-Ortega B,Gaviño-Vergara A,Sáez-de-Ocariz M,Velasco-Hernández Mde L,Salas-Labadía C

更新日期：2014-09-01 00:00:00

abstract：:In addition to the evaluation of melanocytic growths (Part I), dermoscopy is helpful in the identification and management of vascular tumors, skin infections, and inflammatory conditions. In this practical review, we present the classic dermoscopic findings of the following: vascular tumors, infectious conditions (mol...

journal_title：Pediatric dermatology

authors： Natsis NE,Gordon SC,Kaushik A,Seiverling EV

更新日期：2020-09-01 00:00:00

abstract：:Lindane (gamma benzene hexachloride) is a widely prescribed topical scabicide because of its efficacy and cost-effectiveness. Although toxicity from a single proper application of lindane is generally not observed, the hazards of repeated applications, industrial exposure, and accidental ingestion have been well docum...

journal_title：Pediatric dermatology

authors： Bhalla M,Thami GP

更新日期：2004-09-01 00:00:00

abstract：:Acne fulminans is a severe form of acne characterized by painful, inflammatory nodules that progress into ulcers and concurrent systemic symptoms. Treatment of acne with isotretinoin can precipitate a syndrome called isotretinoin-induced acne fulminans without systemic symptoms. An exuberant granulation tissue respons...

journal_title：Pediatric dermatology

authors： Li AW,Antaya RJ

更新日期：2018-03-01 00:00:00

abstract：:Cutaneous xanthomas develop as a result of lipid deposition in the dermis and may be a manifestation of various systemic diseases. The morphology and anatomic location of xanthomas are often a clue to the underlying cause. Xanthoma striatum palmare (XSP) is classically associated with dysbetalipoproteinemia and rarely...

journal_title：Pediatric dermatology

authors： Joner Mattias F,Escobar GF,Peruzzo J

更新日期：2020-09-01 00:00:00

abstract：:We describe a premature neonate who was born with pancytopenia and a single subcutaneous nodule on her right lower extremity. A biopsy specimen from the nodule demonstrated a dense infiltrate of pleomorphic mononuclear cells that extended throughout the dermis and into the subcutaneous tissue. Immunohistochemical stai...

journal_title：Pediatric dermatology

authors： Fender AB,Gust A,Wang N,Scott GA,Mercurio MG

更新日期：2008-01-01 00:00:00

abstract：:Parry-Romberg syndrome (PRS) is characterized by hemiatrophy of facial structures, including skin, subcutaneous fat, muscle, bone, and cartilage. Complications associated with PRS include headaches, seizures, and chronic facial pain. Protocol for the treatment of chronic facial pain is not clear; reports on the use of...

journal_title：Pediatric dermatology

authors： Mishra K,Sood A,Smidt A,Price HN

更新日期：2019-03-01 00:00:00

abstract：:A newborn girl had typical "blueberry muffin" skin lesions, which showed histopathologic features of myelomonocytic leukemia cutis. We could not demonstrate leukemic infiltration of bone marrow in four aspirates. Her course was complicated with primary pulmonary hypertension, which led to death at 7 months of age. We ...

journal_title：Pediatric dermatology

authors： Torrelo A,Madero L,Mediero IG,Baño A,Zambrano A

更新日期：2004-07-01 00:00:00

abstract：:Cerebriform intradermal nevus is a rare form of cutis verticis gyrata. Clinically it manifests as a scalp deformity resembling the surface of the brain, with cerebriform morphologic characteristics. Degeneration into malignant melanoma has been reported. Herein, a cerebriform intradermal nevus of the scalp in a 7-year...

journal_title：Pediatric dermatology

authors： Yazici AC,Ikizoglu G,Baz K,Polat A,Ustunsoy D

更新日期：2007-03-01 00:00:00

abstract：:We describe three teenage siblings with confluent and reticulated papillomatosis, all presenting during a 6-month period. Two of the three patients had confirmed tinea versicolor, with positive potassium hydroxide scrapings, in association with this entity. This is the largest series of siblings with confluent and ret...

journal_title：Pediatric dermatology

authors： Stein JA,Shin HT,Chang MW

更新日期：2005-07-01 00:00:00

abstract：:This study sought to identify barriers to treatment in children with chronic inflammatory skin disease, particularly those with atopic dermatitis, psoriasis, and acne vulgaris. Caregivers of 101 patients seen in the Children's Specialty Group Division of Dermatology, Children's Hospital of The King's Daughters, Norfol...

journal_title：Pediatric dermatology

authors： Ellis RM,Koch LH,McGuire E,Williams JV

更新日期：2011-05-01 00:00:00

abstract：:An 8-year-old girl had Crohn's disease of the vulva 16 months before the onset of intestinal symptoms. At the time of diagnosis she had no evidence of systemic disease. Cutaneous and intestinal lesions responded rapidly to corticosteroids and metronidazole. Crohn's disease must be considered in the differential diagno...

journal_title：Pediatric dermatology

authors： Lally MR,Orenstein SR,Cohen BA

更新日期：1988-05-01 00:00:00

abstract：:Case of an 18-month-old child with congenital lymphedema subsequently diagnosed with tuberous sclerosis and Hirschsprung disease. ...

journal_title：Pediatric dermatology

authors： Lucas M,Andrade Y

更新日期：2011-03-01 00:00:00

abstract：:Condylomata acuminata (CA), or anogenital warts, are typically benign lesions caused by human papillomavirus infection. Although they are rare, immunocompromised individuals are at a higher risk of CA undergoing transformation into invasive anal squamous cell carcinoma (SCC). These patients need aggressive evaluation ...

journal_title：Pediatric dermatology

authors： Paul S,Cheng CE,Kroshinsky D

更新日期：2015-07-01 00:00:00

abstract：:The common manifestations of atopic dermatitis (AD) appear sequentially with involvement of the cheeks in infancy, flexural extremities in childhood, and hands in adulthood. Although less common clinical manifestations are well described, they have not been the subject of epidemiologic studies to describe their preval...

journal_title：Pediatric dermatology

authors： Julián-Gónzalez RE,Orozco-Covarrubias L,Durán-McKinster C,Palacios-Lopez C,Ruiz-Maldonado R,Sáez-de-Ocariz M

更新日期：2012-09-01 00:00:00

abstract：:In 1980 a syndrome was first described in two adult males, consisting of macrocephaly, pigmented macules on the glans and shaft of the penis, and hamartomatous intestinal polyps. Since then, 10 additional cases have been identified. Herein, we present two new cases and review the cutaneous manifestations as well as ad...

journal_title：Pediatric dermatology

authors： Gretzula JC,Hevia O,Schachner LS,DiLiberti JH,Ruvalcaba RH,Schimschock JR,Weleber RG,Halal F,Lipson MH,Blumberg B

更新日期：1988-02-01 00:00:00

abstract：BACKGROUND:Children with congenital melanocytic nevi (CMN) were historically managed with surgical removal to lower the risk of malignant transformation. The evolving literature over the last decade has indicated a significantly lower risk than previously estimated. Indications for excision currently revolve around aes...

journal_title：Pediatric dermatology

authors： Mosa A,Ho ES,Heinelt M,Wong K,Neuhaus K

更新日期：2019-11-01 00:00:00

abstract：:A 5-year-old boy developed hemorrhagic mucocutaneous blisters on various parts of the body leading to fetor, dysphagia, dysuria, anal pruritus, pain on defecation, and weight loss. The histopathology showed the classic features of pemphigus vulgaris, and direct immunofluorescence showed intercellular deposition of IgG...

journal_title：Pediatric dermatology

authors： Bjarnason B,Skoglund C,Flosadóttir E

更新日期：1998-09-01 00:00:00

abstract：:A 15-year-old girl had a new variation of Andogsky syndrome (unilateral cataract and atopic dermatitis) in which atopic dermatitis was associated with primary bilateral cataracts and retinal degeneration with primary left retinal detachment before cataract surgery. She had no history of systemic steroid treatment. ...

journal_title：Pediatric dermatology

authors： Margolin L,Hershko K,Garcia-Rojas M,Ingber A

更新日期：2003-09-01 00:00:00

abstract：:Pulmonary manifestations are well recognized during the acute phase of Stevens-Johnson syndrome but persistent pulmonary sequela is rarely reported. We report two boys with bronchiolitis obliterans following the acute phase of Stevens-Johnson syndrome and discuss the clinical picture and treatment of persistent pulmon...

journal_title：Pediatric dermatology

authors： Bakirtas A,Harmanci K,Toyran M,Razi CH,Turktas I

更新日期：2007-07-01 00:00:00

abstract：:We examined a father and son affected by Ehlers-Danlos syndrome type II. Both patients had micrognathia together with ligament and skin hyperlaxity. The son exhibited complete cleft palate. Ultrastructural studies revealed abnormal collagen fibrils in the dermis of both patients. In the child the most striking alterat...

journal_title：Pediatric dermatology

authors： Rizzo R,Contri MB,Micali G,Quaglino D,Pavone L,Ronchetti IP

更新日期：1987-11-01 00:00:00

abstract：:Phrynoderma is a distinctive form of follicular hyperkeratosis associated with nutritional deficiency. Although originally thought to represent vitamin A deficiency, several studies have demonstrated multiple etiologies. Characteristic skin lesions are hyperkeratotic papules that first appear on the extensor surfaces ...

journal_title：Pediatric dermatology

authors： Maronn M,Allen DM,Esterly NB

更新日期：2005-01-01 00:00:00